FDA Inspection 1025605 — General Cardiac Technology Inc

General Cardiac Technology Inc — FEI 2938604

The FDA completed an inspection of General Cardiac Technology Inc on September 5, 2017 in San Jose, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 5, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Jose, CA (United States)